RecruitingPhase 1NCT06445907

Phase I Study of Q702 With Azacitidine and Venetoclax for Relapsed or Refractory Acute Myeloid Leukemia


Sponsor

M.D. Anderson Cancer Center

Enrollment

32 participants

Start Date

Feb 12, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

To learn about the safety and tolerability of the drug combination of Q702, azacitidine, and venetoclax when given to participants with relapsed/refractory AML.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This early-phase study tests whether adding an experimental drug called Q702 to a standard two-drug combination (azacitidine and venetoclax) is safe and effective in patients with acute myeloid leukemia (AML) — a blood cancer — that has relapsed or stopped responding to previous treatment. **You may be eligible if...** - You are 18 or older with confirmed AML (or a related condition called MDS/AML) that has relapsed or not responded to prior treatment - You have no remaining standard treatment options - You are in good general health (ECOG 0–1) - If you relapsed after a stem cell transplant, you have recovered from transplant-related complications and are off immunosuppression **You may NOT be eligible if...** - You have acute promyelocytic leukemia (a specific subtype of AML) - You have active or uncontrolled infection, or severe organ problems - Your prior remission lasted less than 12 months and you are younger than 60 (unless you have certain high-risk features) Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGAzacitidine

Given by IV

DRUGVenetoclax

Given by PO

DRUGQ702

Given by PO


Locations(1)

MD Anderson Cancer Center

Houston, Texas, United States

View Full Details on ClinicalTrials.gov

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NCT06445907


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